A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6051497



Internal ID21960730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44624152..44624301hg38UCSC Ensembl
chr19:45127449..45127598hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17628880
Samples
Known GenesIGSF23
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6051497
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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